"60505-4058-0" National Drug Code (NDC)

NDC Code	60505-4058-0
Package Description	10 BLISTER PACK in 1 CARTON (60505-4058-0) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC	60505-4058
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nevirapine
Non-Proprietary Name	Nevirapine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20140415
Marketing Category Name	ANDA
Application Number	ANDA205258
Manufacturer	Apotex Corp
Substance Name	NEVIRAPINE
Strength	400
Strength Unit	mg/1
Pharmacy Classes	Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA]